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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PARATHYROID HORMONE Cause Device use error? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Device use error have been filed in association with PARATHYROID HORMONE (NATPARA (parathyroid hormone)). This represents 0.2% of all adverse event reports for PARATHYROID HORMONE.

10
Reports of Device use error with PARATHYROID HORMONE
0.2%
of all PARATHYROID HORMONE reports
1
Deaths
3
Hospitalizations

How Dangerous Is Device use error From PARATHYROID HORMONE?

Of the 10 reports, 1 (10.0%) resulted in death, 3 (30.0%) required hospitalization.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PARATHYROID HORMONE. However, 10 reports have been filed with the FAERS database.

What Other Side Effects Does PARATHYROID HORMONE Cause?

Recalled product (900) Hypocalcaemia (784) Blood calcium decreased (703) Paraesthesia (364) Muscle spasms (357) Headache (257) Drug ineffective (217) Blood calcium increased (212) Nausea (201) Inappropriate schedule of product administration (195)

What Other Drugs Cause Device use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which PARATHYROID HORMONE Alternatives Have Lower Device use error Risk?

PARATHYROID HORMONE vs PARECOXIB PARATHYROID HORMONE vs PARICALCITOL PARATHYROID HORMONE vs PARITAPREVIR PARATHYROID HORMONE vs PAROXETINE PARATHYROID HORMONE vs PAROXETINE\PAROXETINE

Related Pages

PARATHYROID HORMONE Full Profile All Device use error Reports All Drugs Causing Device use error PARATHYROID HORMONE Demographics